Independent recall search Not a government website Verify instructions at the issuing-agency source
FDA source record Class III Ongoing

Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864 0; Manufactured by Renata Restaurant, 626 SE Main St, P...

Recall Date: 2021-10-29 Recalling Firm: Mi Piace LLC Record Ref: F-0279-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864 0; Manufactured by Renata Restaurant, 626 SE Main St, P... and names Mi Piace LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Mi Piace LLC
  • Classification: Class III
  • Status: Ongoing
  • Recall date: 2021-10-29
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

FDA public announcements can appear before an enforcement report is classified, so an empty classification does not mean the notice is unimportant.

Product Description & Identification

Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864 0; Manufactured by Renata Restaurant, 626 SE Main St, Portland, OR 97214; Product label, "Contains Wheat, Milk, Nuts, Coconut"

Reason for Recall / Hazard Identified

Undeclared soy allergen in frozen pizza

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

Verify product details with official government notices before taking action.

Distribution & Affected States

Product was distributed to a distributor in OR who further distributed to 13 New Seasons Market locations in OR and WA.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

Open FDA Source Record →

Record Transparency

Issuing agency
FDA
Source ID
F-0279-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record